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Francisco M. De La Vega
Francisco M. De La Vega
Stanford University School of Medicine
Verified email at stanford.edu - Homepage
Title
Cited by
Cited by
Year
A global reference for human genetic variation
TGP Consortium
Nature 526, 68-74, 2015
12859*2015
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
87172010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
82232012
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1
J Hampe, A Franke, P Rosenstiel, A Till, M Teuber, K Huse, M Albrecht, ...
Nature genetics 39 (2), 207-211, 2007
22942007
Pan-cancer analysis of whole genomes
Nature 578 (7793), 82-93, 2020
1641*2020
Mapping copy number variation by population-scale genome sequencing
RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ...
Nature 470 (7332), 59-65, 2011
12672011
Organoid modeling of the tumor immune microenvironment
JT Neal, X Li, J Zhu, V Giangarra, CL Grzeskowiak, J Ju, IH Liu, SH Chiou, ...
Cell 175 (7), 1972-1988. e16, 2018
10202018
An Aboriginal Australian genome reveals separate human dispersals into Asia
M Rasmussen, X Guo, Y Wang, KE Lohmueller, S Rasmussen, ...
Science 334 (6052), 94-98, 2011
8642011
Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding
KJ McKernan, HE Peckham, GL Costa, SF McLaughlin, Y Fu, EF Tsung, ...
Genome research 19 (9), 1527-1541, 2009
7972009
Diversity of human copy number variation and multicopy genes
PH Sudmant, JO Kitzman, F Antonacci, C Alkan, M Malig, A Tsalenko, ...
Science 330 (6004), 641-646, 2010
7802010
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
7072011
Variation in genome-wide mutation rates within and between human families
Nature genetics 43 (7), 712-714, 2011
6842011
Development of personalized tumor biomarkers using massively parallel sequencing
RJ Leary, I Kinde, F Diehl, K Schmidt, C Clouser, C Duncan, A Antipova, ...
Science translational medicine 2 (20), 20ra14-20ra14, 2010
6702010
Neratinib after trastuzumab-based adjuvant therapy in HER2-positive breast cancer (ExteNET): 5-year analysis of a randomised, double-blind, placebo-controlled, phase 3 trial
M Martin, FA Holmes, B Ejlertsen, S Delaloge, B Moy, H Iwata, ...
The lancet oncology 18 (12), 1688-1700, 2017
6352017
Genomics for the world
CD Bustamante, FM De La Vega, EG Burchard
Nature 475 (7355), 163-165, 2011
6252011
Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America
R Kosoy, R Nassir, C Tian, PA White, LM Butler, G Silva, R Kittles, ...
Human mutation 30 (1), 69-78, 2009
5892009
A high-density admixture map for disease gene discovery in African Americans
MW Smith, N Patterson, JA Lautenberger, AL Truelove, GJ McDonald, ...
The American Journal of Human Genetics 74 (5), 1001-1013, 2004
4782004
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
O Delaneau, J Marchini
Nature communications 5 (1), 3934, 2014
4322014
Integrative annotation of variants from 1092 humans: application to cancer genomics
E Khurana, Y Fu, V Colonna, XJ Mu, HM Kang, T Lappalainen, A Sboner, ...
Science 342 (6154), 1235587, 2013
4232013
A second-generation combined linkage–physical map of the human genome
TC Matise, F Chen, W Chen, M Francisco, M Hansen, C He, FCL Hyland, ...
Genome research 17 (12), 1783-1786, 2007
3522007
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